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Structure of 20949-84-2
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2-Methyl-1,3-thiazole-4-carbaldehyde features a reactive aldehyde group fused to an electron-deficient thiazole ring, enabling direct coupling in heterocyclic synthesis. This bench-stable scaffold integrates readily into medicinal chemistry libraries and serves as a key intermediate for bioactive compound development.
2-Methyl-1,3-thiazole-4-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to biologically relevant thiazole derivatives. Its aldehyde functionality facilitates standard transformations such as reductive amination, Grignard additions, and Wittig reactions, while the methyl-substituted thiazole ring exhibits good bench stability and functional group tolerance. This compound functions effectively in the construction of pharmaceutical scaffolds and agrochemical intermediates through reliable, well-documented reaction pathways.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: